0000000000536099

AUTHOR

Ralph Spallek

showing 3 related works from this author

Sequestration of T lymphocytes to body fluids in tuberculosis: reversal of anergy following chemotherapy.

1999

The specificity of CD4 T lymphocytes was investigated in 6 patients affected by tuberculosis who had negative tuberculin purified protein derivative (PPD) skin tests at diagnosis. Polyclonal CD4 T cell lines from the peripheral blood failed to proliferate to PPD and to the 16- or 38-kDa proteins of Mycobacterium tuberculosis, while CD4 cell lines from the disease site responded to PPD and to the 16- and 38-kDa proteins and derived epitopes in vitro. Four months after chemotherapy, the patients became responsive to PPD. The proliferative response to PPD and to the 16- or 38-kDa proteins and their derived peptides decreased in CD4 T cell lines from the disease site and increased in lines from…

CD4-Positive T-LymphocytesTuberculosisLipoproteinsTuberculinTuberculinEpitopeMycobacterium tuberculosisAntigenImmunology and AllergyMedicineHumansTuberculosisTuberculosis PulmonaryAntibacterial agentClonal AnergyAntigens BacterialClonal anergybiologybusiness.industryT lymphocytebiology.organism_classificationmedicine.diseaseBody FluidsInfectious DiseasesImmunologybusinessThe Journal of infectious diseases
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Broad clonal heterogeneity of antigen-specific CD4+ T-cells localizing at the site of disease during tuberculosis

1999

The repertoire of CD4+ T-lymphocytes was investigated in six patients affected by tuberculosis, who had a negative PPD skin test at diagnosis. Polyclonal CD4+ T-cell lines from the peripheral blood failed to proliferate to PPD and to the 16- or 38-kDa proteins of Mycobacterium tuberculosis, while CD4+ T-cell lines from the site of disease responded to PPD, and to the 16- and 38-kDa proteins, and derived epitopes in vitro. The repertoire of CD4+ T-cells accumulating at the site of disease was found to be widely heterogeneous as demonstrated by the finding that at least seven different peptides from the 16- and 38-kDa proteins were recognized by every patient. These results indicate that CD4+…

CD4-Positive T-LymphocytesTuberculosisLipoproteinsMolecular Sequence DataImmunologyEpitopes T-LymphocyteDiseaseEpitopeMeningitis BacterialMycobacterium tuberculosisAntigen specificmedicineHumansTuberculosisImmunology and AllergyAmino Acid SequencePleurisyAntigens BacterialbiologyRepertoireMycobacterium tuberculosisPericarditis Tuberculousbiology.organism_classificationmedicine.diseaseVirologyIn vitroPolyclonal antibodiesImmunologybiology.proteinImmunology Letters
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Change of Th0 to Th1 cell-cytokine profile following tuberculosis chemotherapy.

2000

T cells mediate protection against tuberculosis, but little is known about their role during chemotherapy of patients with active disease. Here we examined the cytokine profile of CD4 T cells before and after four months of chemotherapy in six initial skin test anergic cases. Purified protein derivative (PPD) and 16-kDa antigen-reactive CD4 T-cell clones prior to therapy resided mostly in disease-associated body fluids and were of the Th0 (interferon (IFN)-gamma + interleukin (IL)-4) secreting profile. In contrast, the majority of postchemotherapy CD4 T-cell clones originated from blood and were of the IFN-gamma secreting Th1 type. However, the recognition of several peptides derived from t…

CD4-Positive T-LymphocytesTuberculosisTuberculosis chemotherapyCytokine profilemedicine.medical_treatmentImmunologyCellLymphocyte ActivationTuberculinInterferon-gammaTh2 CellsAntigenInterferonmedicineHumansTuberculosisChemotherapybusiness.industryInterleukinGeneral MedicineTh1 Cellsmedicine.diseaseCrystallinsmedicine.anatomical_structureImmunologyInterleukin-4businessmedicine.drugScandinavian journal of immunology
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